The Recall Desk

State

Illinois product recalls

73,092 recalls have nationwide distribution and so reach Illinois. 11,640 additional recalls listed Illinois specifically in their distribution scope.

What the numbers show

Total
11,640
Critical
2,049
Severe
2,533
Most recent
2026-09-25

Of the 11,640 recalls naming Illinois we have scored against our rubric, 2,049 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,533 (22%) are Severe.

These figures cover only the 11,640 recalls whose distribution notice names Illinois specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9351–9375 of 84732

  • HighNHTSA·24V931000·2024-12-13

    Featherlite Recalls 2023-2024 Horse Trailers Due to Fire Risk

    Featherlite is recalling 2023-2024 Living Quarters Horse Trailers because a rubber gas line may overheat and cause a fire. Dealers will install a copper extension free of charge.

    Product
    FEATHERLITE — FEATHERLITE 9807, 7841, 9808, 7821
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25066·2024-12-12

    HTRC C240 Battery Chargers Recalled for Fire and Burn Hazards

    HTRC C240 battery chargers may ignite or cause connected batteries to ignite, posing fire and burn hazards. The recall affects about 34,600 units sold online from December 2017 through June 2024.

    Product
    HTRC C240 battery chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25063·2024-12-12

    Stanley Recalls 2.6 Million Travel Mugs for Burn Hazard

    Stanley is recalling 2.6 million Switchback and Trigger Action travel mugs whose lids can detach during use, causing burn injuries. The company has received 91 reports worldwide (16 in the U.S.) of lid detachment resulting in 38 burn injuries, with 11 requiring medical attention.

    Product
    Switchback and Trigger Action travel mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V926000·2024-12-12

    2024 Jeep Grand Cherokee Radiator Crossmember Bolts May Not Be Properly Secured

    Chrysler is recalling 631 units of the 2024 Jeep Grand Cherokee and Grand Cherokee L due to unsecured radiator crossmember bolts that may cause improper airbag deployment and fuel leaks during crashes, increasing injury and fire risks.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25064·2024-12-12

    Wall Teester Bed Crowns Recalled Due to Mounting Tab Failure

    Touch of Class is recalling about 890 Wall Teester Bed Crowns because their welded mounting tabs can weaken and fail, causing the crown to fall from the wall. One injury has been reported.

    Product
    Wall Teester Bed Crowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V925000·2024-12-12

    2025 Chevrolet Equinox EV Pedestrian Alert Sound System Defect

    General Motors is recalling 7,606 2025 Chevrolet Equinox EV vehicles due to incorrect pedestrian alert sound software that fails to produce sufficient volume. This violates federal safety standards and may increase the risk of pedestrian injury.

    Product
    CHEVROLET — CHEVROLET EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25065·2024-12-12

    Yoto Mini speakers recalled for battery fire and burn hazards

    Yoto Inc. is recalling approximately 251,165 Yoto Mini speakers because the lithium-ion battery can overheat and catch fire. No injuries have been reported, but consumers should stop using the product and contact Yoto for a free battery replacement kit.

    Product
    Yoto Mini speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25067·2024-12-12

    Wireless Tree Light Controllers Recalled Due to Fire Hazard

    Wireless tree light controllers sold at Walmart, Target, and Cracker Barrel are being recalled because the receiver can overheat and catch fire. Ten overheating incidents and one fire have been reported, with no injuries.

    Product
    Wireless Decorative Tree Light Controllers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0248-2025·2024-12-11

    Albertsons Ready-Meal Salads Recalled for Listeria Contamination

    Albertsons Companies LLC recalls multiple ready-meal salad products due to Listeria monocytogenes contamination in cooked chicken. Products were distributed across 21 US states with sell-through dates through October 13, 2024.

    Product
    (1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) READY MEALS GINGER CHICKEN BROCOLLI SALAD SS (UPC 29105700000) (3) GINGER BROCOLLI SALAD FS (UPC 29233600000) (4) CHICKEN CAESAR SALAD FS (UPC 29130700000) (5) CAESAR CHICKEN BOWL (UPC 29125500000) (6) READY MEALS CHICKEN
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Food)·F-0257-2025·2024-12-11

    Fresh Express Salad Bowls Recalled for Potential Listeria Contamination

    Fresh Express Gourmet Cafe Santa Fe Greek salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a chicken ingredient recall. No illnesses have been reported.

    Product
    Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·24E104000·2024-12-11

    ATP Recalls Air Brake Tubing Due to Bursting Risk

    Advanced Technology Products is recalling specific air brake tubing that may crack and burst under pressure, potentially causing a loss of braking ability.

    Product
    SERVICE BRAKES, AIR:SUPPLY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0083-2025·2024-12-11

    VitalityXtra Capsules Recalled for Undeclared Sildenafil and Diclofenac

    VitalityXtra Capsules containing undeclared sildenafil and diclofenac are being recalled nationwide. The product was marketed without required FDA approval and poses health risks from undeclared pharmaceutical ingredients.

    Product
    VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0086-2025·2024-12-11

    ZapMax Capsules Recalled for Undeclared Sildenafil and Diclofenac

    ZapMax Capsules, 500 mg are recalled for containing undeclared sildenafil and diclofenac without FDA approval. The product was distributed nationwide; consumers should stop using immediately and consult their healthcare provider.

    Product
    ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0085-2025·2024-12-11

    ZoomMax Capsules contain undeclared sildenafil and diclofenac

    ZoomMax Capsules have been recalled by the FDA due to containing undeclared sildenafil and diclofenac. The product was marketed without FDA approval.

    Product
    ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0084-2025·2024-12-11

    PeakMax Capsules Recalled for Undeclared Sildenafil and Diclofenac

    PeakMax Capsules contain undeclared sildenafil and diclofenac and were marketed without FDA approval. This Class I recall affects capsules distributed nationwide.

    Product
    PeakMax Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: PeakMax, San Francisco, CA, www.PeakMax.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0256-2025·2024-12-11

    Fresh Express Chicken Caesar Salad Bowls Recalled for Listeria Monocytogenes

    Fresh Express Gourmet Cafe Chicken Caesar salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a Bruce Pac recall. The recall affects products distributed across multiple U.S. states.

    Product
    Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279407074 and Case Code:071279565620
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·24V924000·2024-12-11

    Freightliner M2 Emergency Vehicles Recalled for Engine Shutdown Risk

    Daimler Trucks is recalling 2015-2020 Freightliner Business Class M2 emergency vehicles because software may cause unexpected engine shutdowns, delaying responders.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0090-2025·2024-12-11

    ROYALAB Germ Away Antibacterial Hand Soap Recalled for Failed Microbiological Testing

    Midlab Incorporated is recalling ROYALAB Germ Away Antibacterial Hand Soap (1-gallon, Lot 0711241) due to out-of-specification microbiological test results. The product failed manufacturing quality standards.

    Product
    ROYALAB Germ Away Antibacterial Hand Soap, Chloroxylenol 0.1%, NET CONTENTS: ONE U.S. GALLON (3.78 L), Royal Papers, 2701 Hereford St., St. Louis, MO 63139
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0620-2025·2024-12-11

    Olympus Removes Acecide-C Disinfection from GIF-1TH190 Endoscope Reprocessing

    Olympus has removed high-level disinfection with Acecide-C as an approved reprocessing method for the GIF-1TH190 gastrointestinal videoscope. Approximately 1,770 units nationwide are affected.

    Product
    EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0598-2025·2024-12-11

    Cartiva Synthetic Cartilage Implants Recalled Due to Higher Complication Rates

    Cartiva Synthetic Cartilage Implants are being recalled due to higher-than-expected rates of complications including implant displacement, subsidence, nerve damage, and fragmentation. Patients with these implants should consult their surgeon.

    Product
    Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0649-2025·2024-12-11

    Medline recalls surgical kits containing Stryker smoke evacuation pencil component

    Medline is recalling medical convenience kits containing SafeAir Smoke Evacuation Pencils that were previously recalled by Stryker.

    Product
    MEDLINE convenience kits labeled as: 1) ORTHO LAMINECTOMY-LF, REF CDS780112J; 2) NEURO CRANIOTOMY CDS #36-RF, REF CDS780119V; 3) BASIC BACK CDS, REF CDS780147N; 4) INSTRUMENTED BACK CDS, REF CDS780148Q; 5) INSTRUMENTED BACK CDS, REF CDS780148R; 6) TOTAL HIP, REF CDS920027W
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0222-2025·2024-12-11

    AROMA VITA Hot Cocoa Mix Recalled for Metal Fragments

    AROMA VITA Hot Cocoa Mix is being recalled due to metal fragments in the product caused by a damaged sifter used during dextrose production.

    Product
    AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA Brands, Inc. Atlanta, GA 30328
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0226-2025·2024-12-11

    Gordon CHOICE Lemonade Mix Recalled for Metal Fragment Contamination

    Gordon CHOICE Lemonade Beverage Mix is being recalled for metal fragment contamination in the product. Consumers should stop using affected packages and contact the manufacturer.

    Product
    Gordon CHOICE Lemonade Beverage Mix Naturally Flavored Low Calorie Instant LOW CAL LEMONADE, NET WT. 8.6 OZ (243 g), UPC 0 93901 59605 5, Case UPC 10093901596052, FOR DISTRIBUTION EXCLUSIVELY BY PARA SU DISTRIBUCION EXCLUSIVA POR GORDON FOOD SERVICE WYOMING, MI 49509
    Category
    Food
    Distribution
    30 states